Canonical Allele Identifier: CA1003892032
Gene: PRKACB HGNC NCBI

Linked Data

dbSNP Id: rs1649298890
gnomAD v3: 1-84100843-A-T
gnomAD v4: 1-84100843-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.84100843A>T , CM000663.2:g.84100843A>T GRCh38
NC_000001.10:g.84566526A>T , CM000663.1:g.84566526A>T GRCh37
NC_000001.9:g.84339114A>T NCBI36
NG_029728.1:g.27782A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370688.7:c.46+22472A>T ENSP00000359722.3:n.46+22472A>T
ENST00000370689.6:c.46+22472A>T ENSP00000359723.2:n.46+22472A>T
NM_002731.3:c.46+22472A>T NP_002722.1:n.46+22472A>T
NM_207578.2:c.46+22472A>T NP_997461.1:n.46+22472A>T
XM_011541764.1:c.46+22472A>T XP_011540066.1:n.46+22472A>T
XM_017001713.2:c.46+22472A>T XP_016857202.1:n.46+22472A>T
NM_001375576.1:c.46+22472A>T NP_001362505.1:n.46+22472A>T
NM_207578.3:c.46+22472A>T NP_997461.1:n.46+22472A>T
NM_002731.4:c.46+22472A>T NP_002722.1:n.46+22472A>T